• Senior Manager, Pharmacovigilance Scientist

    Sumitomo Pharma (Raleigh, NC)
    …. **Job Overview** The Senior Manager, Pharmacovigilance Scientist serves as the primary ... and at partner meetings including Joint Safety Forums (JSFs) and Pharmacovigilance Committee (PVC) meetings. + Review adverse event reports-including serious… more
    Sumitomo Pharma (06/28/25)
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  • Associate Medical Director,…

    Sumitomo Pharma (Raleigh, NC)
    …+ Knowledge of ICH, US & EU regulations, and requirements for Pharmacovigilance . + Excellent interpersonal skills, with demonstrated ability to work in a ... Experience in oncology is highly desired + **Advanced understanding of pharmacovigilance and risk management regulations and guidelines, including pre- and… more
    Sumitomo Pharma (05/16/25)
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  • Senior Global Patient Safety Quality, Training…

    United Therapeutics (Raleigh, NC)
    …You have a background in nursing or pharmacy and you're passionate about pharmacovigilance ! You are a team player who loves quality, compliance, finding solutions ... practices. They will serve as a Subject Matter Expert for pharmacovigilance (PV), quality practices, education/training, and audits/inspections to support both… more
    United Therapeutics (07/12/25)
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  • Manager, PVRM

    Sumitomo Pharma (Raleigh, NC)
    …a dynamic, highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). Ability to ... ongoing clinical trials. + Serve as a subject matter expert in Pharmacovigilance , including operations and medical, within the assigned program. + Support… more
    Sumitomo Pharma (08/01/25)
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  • Safety Specialist

    IQVIA (Durham, NC)
    …+ Assist with business partner and other query management. + Represent Pharmacovigilance on project teams. + Assist with CAPA/audit or inspection finding ... of data to support quality and compliance processes. + Assist with Pharmacovigilance reconciliation of databases and listings (post marketing and clinical trial… more
    IQVIA (07/31/25)
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  • Global Patient Safety Affiliate, Alliance,…

    United Therapeutics (Research Triangle Park, NC)
    …an option. **Who You Are** Do you have a deep understanding of pharmacovigilance (PV) regulations globally and their operational implications for a wide range of ... This role is responsible for management of Global Product Safety & Pharmacovigilance business alliance activities and contribution to AA&C projects and initiatives.… more
    United Therapeutics (05/17/25)
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  • Senior Product Safety Scientist

    United Therapeutics (Research Triangle Park, NC)
    …We are seeking an experienced Senior Product Safety Scientist to join our dynamic pharmacovigilance team. You will play a key role in managing the safety profile of ... data from a safety perspective + Intermediate to advanced knowledge of pharmacovigilance processes and regulatory requirements + Advanced knowledge of MedDRA coding… more
    United Therapeutics (08/01/25)
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  • Medical Director, Gastroenterologist

    IQVIA (Durham, NC)
    …review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. + May provide medical support for the Analysis of Similar ... Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. + May perform medical review of adverse event coding. + Performs review of the… more
    IQVIA (07/24/25)
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  • Reimbursement Case Manager

    TEKsystems (Morrisville, NC)
    …and regulations for the programs/promotions + Identify and report pharmacovigilance information as required by client(s)(ie, Adverse Events)-(specific to ... + Conducts miscellaneous tasks or projects as assigned. Identify and report pharmacovigilance information as required by client(s) (ie, Adverse Events) - (specific… more
    TEKsystems (07/22/25)
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  • Associate Medical Director/Medical Director…

    ThermoFisher Scientific (Greenville, NC)
    …find cures for cancer. **Location/Division Specific Information** Our detailed, goal-oriented Pharmacovigilance colleagues manage the safety profile of new drugs in ... to 1-2 years) in the industry; Or + Direct experience in safety/ Pharmacovigilance (comparable to 2 years) + Experience preference towards individuals with clinical… more
    ThermoFisher Scientific (07/15/25)
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